z-logo
open-access-imgOpen Access
Evidence for a role of vertebrate Disp1 in long-range Shh signaling
Author(s) -
Letitiah Etheridge,
Timothy Q. Crawford,
Shile Zhang,
Henk Roelink
Publication year - 2009
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.043547
Subject(s) - biology , sonic hedgehog , microbiology and biotechnology , hedgehog signaling pathway , transmembrane protein , mesoderm , secretion , embryonic stem cell , precursor cell , embryoid body , hedgehog , signal transduction , cell , genetics , gene , endocrinology , receptor , adult stem cell
Dispatched 1 (Disp1) encodes a twelve transmembrane domain protein that is required for long-range sonic hedgehog (Shh) signaling. Inhibition of Disp1 function, both by RNAi or dominant-negative constructs, prevents secretion and results in the accumulation of Shh in source cells. Measuring the Shh response in neuralized embryoid bodies (EBs) derived from embryonic stem (ES) cells, with or without Disp1 function, demonstrates an additional role for Disp1 in cells transporting Shh. Co-cultures with Shh-expressing cells revealed a significant reduction in the range of the contact-dependent Shh response in Disp1(-/-) neuralized EBs. These observations support a dual role for Disp1, not only in the secretion of Shh from the source cells, but also in the subsequent transport of Shh through tissue.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom